Tonsil/Adenoid/Appendix Drops 5030 NDC 63083-5030

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-5030Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-5030Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
63083-5030-2	63083503002	59 mL in 1 BOTTLE, DROPPER (63083-5030-2)Marketed from Aug 15, 1985

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Tonsil/Adenoid/Appendix Drops 5030Suffix: 5030
Generic name (nonproprietary): tonsil/adenoid/appendix drops
Active ingredients: Berberis aquifolium root bark — 3 [hp_X]/59mLEchinacea angustifolia whole — 3 [hp_X]/59mLSus scrofa lymph — 6 [hp_X]/59mLSus scrofa colon — 6 [hp_X]/59mLBos taurus tonsil — 6 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Identifiers: Product ID 63083-5030_de7246b2-a14c-48ac-b52f-92ae7fc6e020SPL ID de7246b2-a14c-48ac-b52f-92ae7fc6e020SPL set ID 38dbb7f0-9a61-43bf-bc74-fef0b82a7c93UNII VZJ9F3C3SB, VB06AV5US8, 33A7VYU29L, 94J255A0UC, 12SEC09GR1

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083503002 followed by a unit qualifier and the quantity

Package 63083-5030-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of minor sore throat, cough, occasional headache, runny nose, mild abdominal pain, nausea or vomiting, loss of appetite, tiredness, or feelings of discomfort or uneasiness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)